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Scanning transmission X-ray microscopy studies of electrochemical activation and capacitive behavior of Mn 3 O 4 supercapacitor electrodes

Abstract

For the first time scanning transmission X-ray microscopy is used for analysis of activation and charging mechanism of Mn 3 O 4 supercapacitor electrodes. This investigation, which is motivated by promising pseudocapacitive properties of Mn 3 O 4 for energy storage in cathodes of supercapacitors, addresses the need to understand both the activation and the charge storage mechanisms of Mn 3 O 4 electrodes. Specific activation protocols are shown to result in significant capacitance increase during cycling. For the first time scanning transmission X-ray microscopy (STXM) is used for analysis of Mn 3 O 4 activation. STXM analyses at the Mn 2p and O 1s edges provide chemical mapping of different oxidation states with high spatial resolution. Mn 3 O 4 -carbon nanotube composite electrodes with commercially important high active mass loading of 40 mg cm −2 are prepared using quercetin dispersant. The catecholate type polyaromatic quercetin facilitates co-dispersion of Mn 3 O 4 with carbon nanotubes and allows enhanced electrode performance at high active mass loadings. Cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic charge–discharge are used for the capacitance monitoring during electrode activation. Two strategies are used for electrode activation in Na 2 SO 4 electrolyte: electrochemical cycling at different scan rates and continuous cycling at a fixed scan rate. The capacitance variations are linked to STXM observations, which show gradual oxidation of Mn 3 O 4 to form MnO 2 on the particle surface and in the bulk. The pseudocapacitive charge storage mechanism involves in situ oxidation of Mn 3 O 4 and redox reactions of Mn 4+ /Mn 3+ species on the particle surface and in the bulk.

Authors

Yang W; Eraky H; Zhang C; Hitchcock AP; Zhitomirsky I

Journal

Journal of Materials Chemistry A, Vol. 10, No. 35, pp. 18267–18277

Publisher

Royal Society of Chemistry (RSC)

Publication Date

September 13, 2022

DOI

10.1039/d2ta04702k

ISSN

2050-7488

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